XL2013-cell-colony-formation-assay: Difference between revisions
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Xiao Liang - Bergen 2013 - Single cell colony formation assay - 48 well plate |
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Xiao 2013, Bergen | Xiao 2013, Bergen | ||
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Latest revision as of 03:09, 30 August 2018
Single cell colony formation assay #48 well plate
- Typsinize the cells into single cell suspension and put 2ml of cell suspension into 35mm dish (cell density can be adjusted to make it easy to collect the single cells)
- Pick single cells by using 10ul pipette (2ul); or cells were seeded directly into 96-well plates by using the single cell plate sorting function of the FACS Aria sorter (BD biosciences).
- Wells were examined microscopically and those containing only a single clone were selected for analysis.
- Stained with 0.5% crystal violet:
- remove the medium
- wash with PBS once
- add ethonal for 10min with lid on
- open the lid and dry in the air completely
- add 500 ul 0.5% crystal violet for 15 min
- wash with water and dry it
- Count the colony and calculate the colony formation efficiency:
no. of colony /48 *100%
Colony formation assay #6 well plate
- Typsinize the cells into single cell suspension and put a total of 500 cells/well were seeded in 6-well plates within 3 mL complete culture medium in 6 well plate
- Wells were examined microscopically after 7-10 days,
- Stained with 0.5% crystal violet:
- remove the medium
- wash with PBS once
- add ethonal for 10min with lid on
- open the lid and dry in the air completely
- add 500 ul 0.5% crystal violet for 15 min
- wash with water and dry it
- Count the colony and calculate the colony formation efficiency:
no. of colony /500 *100%
Xiao 2013, Bergen